Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000775366 | SCV000909667 | likely benign | Hereditary cancer-predisposing syndrome | 2021-03-19 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002068520 | SCV002434480 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2023-12-12 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV004001450 | SCV004830110 | likely benign | Lynch syndrome | 2023-06-08 | criteria provided, single submitter | clinical testing |